HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2248354Generated: October 31, 2026
Iodine → α-3-Buten-1-yl-2,4-difluorobenzenemethanol
https://huagongshe.com/reaction/2248354
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Homoallyl bromide | HCID 21241 | — |
| Reactant | 2,4-Difluorobenzaldehyde | HCID 73770 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | α-3-Buten-1-yl-2,4-difluorobenzenemethanol | HCID 14994860 | — |
Reaction Steps
To a stirred suspension of magnesium turnings (16.9 gm) in dry diethyl ether (1.5L) was added (argon atmosphere) a crystal of iodine and 4-bromobutene (2 ml). Soon after the reaction was initiated the remaining 4-bromobutene (101 gm) in dry diethyl ether (500 mL) was added at such a rate to maintain gentle reflux. After complete addition, the mixture was heated to reflux for 1 hour. 2,4-Difluorobenzaldehyde (100 gm) in dry diethyl ether (400 mL) was then added dropwise with a gentle reflux. The mixture was now heated for 2 hours and allowed to cool to room temperature. The entire contents of the flask were poured on 6L ice-water containing 200 ml concentrated HCl. The organic phase was separated, washed with water, saturated NaHCO3, water and dried (Na2SO4). Removal of ether in vacuo provided crude 5-hydroxy-5-(2,4-difluorophenyl)pentene as an oil (136.5 gm) which was used in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05039676 |
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| Source dataset | uspto-grants-1991_08 |
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| ORD ID | ord-d8008988cc3c4c2c959e4e070e990700 |
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| Source note | uspto-grants-1991_08 |
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